Introduction to Bioinformatics using NGS data

Topics at this 2 ECTS course organized by SciLifeLab include:

  • Basic Linux usage
  • NGS read-to-reference alignment (genomic and RNA-Seq)
  • Variant calling in populations
  • De novo assembly of RNA-sequence data
  • Reference-guided RNA-Seq expression analysis

Analysis techniques covered will focus mostly on data from the Illumina platform, but other sequencing platforms and the advantages and challenges to using their data will be discussed.

Course fee: 1800 SEK

Application deadline: 13 August, 2017

Link to information about the course at SciLifeLab.

Link to application form (via SciLifeLab)

If you are admitted to the course (after applying via SciLifeLab above) you can apply for co-funding of travel/accommodation costs for participating in the course by filling out the form below. No co-funding is provided with respect to the course fee.


Bookings are closed for this event.